Allele Registry

Canonical Allele Identifier: PA2826616151

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001327086

ClinVar Variation:

1026613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265843.1:p.Gly596Arg	CA367889574 NM_001278914.2:c.1786G>C CA367889575 NM_001278914.2:c.1786G>A